Canonical Allele Identifier: CA1467350184
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71743637C= , CM000666.2:g.71743637C= GRCh38
NC_000004.11:g.72609354C= , CM000666.1:g.72609354C= GRCh37
NC_000004.10:g.72828218C= NCBI36
NG_012837.2:g.66884G=
NG_012837.3:g.66884G=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*26-1767G= MANE Select ENSP00000273951.8:n.*26-1767G=
ENST00000273951.12:c.*26-1767G= ENSP00000273951.8:n.*26-1767G=
ENST00000503364.5:n.124-1767G=
ENST00000503472.5:n.1335-1767G=
ENST00000504199.5:c.*26-1767G= ENSP00000421725.1:n.*26-1767G=
ENST00000509740.5:c.*274-1767G= ENSP00000422664.1:n.*274-1767G=
ENST00000513476.5:c.1396-1767G= ENSP00000426683.1:n.1396-1767G=
NM_000583.3:c.*26-1767G= NP_000574.2:n.*26-1767G=
NM_001204306.1:c.*26-1767G= NP_001191235.1:n.*26-1767G=
NM_001204307.1:c.*26-1767G= NP_001191236.1:n.*26-1767G=
XM_006714177.2:c.*40-1767G= XP_006714240.1:n.*40-1767G=
XM_006714177.3:c.*40-1767G= XP_006714240.1:n.*40-1767G=
NM_000583.4:c.*26-1767G= MANE Select NP_000574.2:n.*26-1767G=